Endonasal endoscopic surgery for temporal lobe epilepsy associated with sphenoidal encephalocele

Author:

Mukae Nobutaka1,Kuga Daisuke1,Murakami Daisuke2,Komune Noritaka2,Miyamoto Yusuke2,Shimogawa Takafumi1,Sakata Ayumi3,Shigeto Hiroshi4,Iwaki Toru5,Morioka Takato6,Mizoguchi Masahiro1

Affiliation:

1. Department of Neurosurgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

2. Department of Otorhinolaryngology Head and Neck Surgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

3. Department of Clinical Chemistry and Laboratory Medicine, Kyushu University Hospital, Fukuoka, Japan.

4. Department of Health Sciences, Graduate School of Medical Sciences, Kyushu University,Fukuoka, Japan.

5. Department of Neuropathology, Graduate School of Medical Sciences, Kyushu University,Fukuoka, Japan.

6. Department of Neurosurgery, Harasanshin Hospital, Fukuoka, Japan.

Abstract

Background: Temporal lobe epilepsy (TLE) associated with temporal lobe encephalocele is rare, and the precise epileptogenic mechanisms and surgical strategies for such cases are still unknown. Although the previous studies have reported good seizure outcomes following chronic subdural electrode recording through invasive craniotomy, only few studies have reported successful epilepsy surgery through endoscopic endonasal lesionectomy. Case Description: An 18-year-old man developed generalized convulsions at the age of 15 years. Despite treatment with optimal doses of antiepileptic drugs, episodes of speech and reading difficulties were observed 2–3 times per week. Long-term video electroencephalogram (EEG) revealed ictal activities starting from the left anterior temporal region. Magnetic resonance imaging revealed a temporal lobe encephalocele in the left lateral fossa of the sphenoidal sinus (sphenoidal encephalocele). Through the endoscopic endonasal approach, the tip of the encephalocele was exposed. A depth electrode was inserted into the encephalocele, which showed frequent spikes superimposed with high-frequency oscillations (HFOs) suggesting intrinsic epileptogenicity. The encephalocele was resected 8 mm from the tip. Twelve months postoperatively, the patient had no recurrence of seizures on tapering of the medication. Conclusion: TLE associated with sphenoidal encephalocele could be controlled with endoscopic endonasal lesionectomy, after confirming the high epileptogenicity with analysis of HFOs of intraoperative EEG recorded using an intralesional depth electrode.

Publisher

Scientific Scholar

Subject

Neurology (clinical),Surgery

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